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Testing & Quality Assurance in San Pedro Arriba

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San Pedro Arriba

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Location:San Pedro Arriba

Category:Testing & Quality Assurance

Specialist CSX CoE Delivery Enablement65110217424001120

Specialist CSX CoE Delivery Enablement

#### **About this Position** The CSX Specialist is responsible for supporting customer operations by managing purchase orders, coordinating inventory and shipping activities, and ensuring timely and accurate order fulfillment. This role serves as a key point of contact between customers, sales, supply chain, and logistics, contributing to a high level of customer satisfaction while maintaining efficient internal processes.**We kindly request to upload your resume in English.** #### **What you´ll do** * Accountable for complex decision related to service delivery activities without direct customer interaction; adopt customer centricity mindset. * Responsible for automated/manual delivery creation/modification/monitoring (delivery block checks, incomplete deliveries/error logs) * Orchestrate/ prioritize customer needs vs. Supply Chain capabilities to fulfill customer/ intercompany orders, while minimizing costs. * Contribute to the understanding Voice of Customer/ trends/ needs/ hurdles; support by providing relevant/accurate service delivery info. * Enter relevant data in the CRM system to create call plan \& ensure quality data for business development activities, schedule follow\-ups. * Provide a quality service to customers indirectly, supporting the identification of opportunities to secure new business or support retention. * Collaborate closely with internal partners (CSX, CoE, GBS\+, SC), judging and aligning priorities to meet customer needs vs. SC capabilities. * Support the implementation of organizational changes, processes, projects, pilots and regional best practices. * Contribute to identifying continuous improvement opportunities to enhance efficiencies, streamline workflows or improve customer experience. * Prioritize own workflow, ensure work is completed with productivity, quality \& timeliness; use KPI's and reports to monitor own performance. * Utilize customer service systems and tools (SAP \& Service Cloud), driving efficiencies and providing feedback to contribute to improvement. #### **What makes you a good fit** * Bachelor’s degree in Business Administration, Supply Chain, or a related field. * 2\+ years of experience in similar positions. * Experience handling purchase orders and customer\-facing processes is preferred. * Basic to intermediate knowledge of SAP and Salesforce; beginner level candidates with strong learning capability are welcome. * Understanding of inventory management and shipping processes. * Strong organizational skills and attention to detail. * Advanced english. #### **Some perks of joining Henkel** * Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year * Diverse national and international growth opportunities * Global wellbeing standards with health and preventive care programs * Gender\-neutral parental leave for a minimum of 8 weeks * Employee Share Plan with voluntary investment and Henkel matching shares * Flexible Benefits * Meal vouchers * Savings fund * Friday early finish At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We welcome all applications across different genders, origins, cultures, religions, sexual orientations, disabilities, and generations.

Nicolás Bravo 5, Centro, 52760 Huixquilucan de Degollado, Méx., Mexico

Supply Chain & Procument Lead65110048193665121

Supply Chain & Procument Lead

Kapsch is one of Austria's most successful global technology companies. With its comprehensive ITS (Intelligent Transportation Systems) portfolio, Kapsch is actively addressing the challenges of the present and the future with intelligent mobility solutions in a wide range of application areas. As a family\-owned company founded in 1892 and headquartered in Vienna, Kapsch can look back on 130 years of experience with the future. **Please attach your CV in English.** We are looking for a **Supply Chain \& Procurement Lead** to join our team! **Your responsibilities:** * Oversee all logistics operations within the country/Subregion LAM. * Analyze statistical data and reports to identify performance trends and drive improvements. * Supervise inventory management of materials, goods, and equipment within the country/Subregion LAM. * Proactively address performance challenges to support seamless operations. * Coordinate transportation and distribution of equipment and materials. * Manage material planning efforts with direct oversight of international and local sourcing. * Develop and execute a comprehensive supply plan, integrating inputs from demand planning, production capacity, and component availability. * Ensure efficient supply chain services, including material planning, scheduling, and strict inventory control for immediate availability. * Review purchasing decisions, orders, and contracts to ensure timely fulfillment and resolve discrepancies promptly to maintain quality and company reputation. * Conduct and present performance evaluations, including disciplinary actions and performance improvement initiatives. * Implement effective inventory control measures to optimize stock levels. * Act as the owner of all local supply chain management (SCM) processes and procedures. * Ensure compliance with internal and external audits, including legal, environmental, and supplier audits when required. **Your profile:** * Previous experience in Procurement/Supply Chain \& Imports, preferably in IT, construction, telecommunications, energy, or related industries. * Advanced English (oral and written). * University degree in Business Administration, Supply Chain, or a related field. * Key Skills: Proactive mindset, excellent communication, negotiation, and problem\-solving skills. * Proficiency in ERP systems and advanced Office Suite. * Willingness to travel within the LAM region when needed. **Our offer to you:** * A full\-time, interesting position within a globally recognized family\-owned company. * Excellent working environment. * An international workplace setting. * Outstanding benefits. **Please attach your CV in English.**

Guanajuato 54, Roma Nte., Cuauhtémoc, 06700 Ciudad de México, CDMX, Mexico

Associate Specialist, Logistics Operations65110048113410122

Associate Specialist, Logistics Operations

Overview: The Associate Specialist, Logistics Operations will execute delivery and logistics activities by transportation mode of packed Goods, liquid or Bulk ensuring on time shipment from the plants/warehouses and on time delivery to the customer. Position will be responsible for day to day SAP transactions in addition to resolving any transportation delays, equipment challenges or other issues impacting on time delivery to the customer. Responsibilities: * Coordinate all load and shipment processes with local plant / warehouse / terminal personnel and carriers to ensure on time delivery to customer * Proactively monitor open orders and deliveries to avoid and resolve issues at the earliest possibility and mitigate negative impact of unavoidable disturbances * Key transactional contact for customers and 3rd party logistics service providers * Ensure adherence to defined operational escalation process to leads, regional experts and plant personnel when encountering unforeseen delays in shipping from plant and ultimate delivery to customer. Manage exceptions and emergency situations * Assist with resolution of freight invoice discrepancies * Document, investigate and follow up of internal and external complaints * Recommend process improvement including investigation of quality failures and the development of preventive and corrective actions for quality failures * Maintain key internal relationships including business, sales, supply chain planning, logistics procurement, product management and further functions. * Run regular (weekly, monthly, quarterly) operational and KPI reports, share findings and trend with leadership, suggest potential improvement ideas where necessary * Meet/exceed monthly KPI metrics and objectives Qualifications: * Bachelor’s degree in a relevant field * 2\-3 years of experience in Logistics Operations or Supply Chain Management * Proficient in English, both written and spoken * Hands\-on experience with SAP or similar ERP systems * Strong customer\-focused mindset with a commitment to service excellence * Results\-driven with a proven ability to meet deadlines and achieve targets * Sound decision\-making skills with the ability to act promptly and effectively * Excellent time management and organizational abilities * Strong troubleshooting and problem\-solving skills * Proven ability to build and maintain effective working relationships * Comfortable working in a fast\-paced, global, and complex environment * Flexible and adaptable to change, with a positive attitude toward continuous improvement * Resilient under pressure and able to manage stress effectively * High level of responsibility, engagement, and ownership of tasks

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

BANAMEX - Consumer Risk Model Management - VP65110048097665123

BANAMEX - Consumer Risk Model Management - VP

The Model/Anlys/Valid Sr Mgr accomplishes results through the management of professional team(s) and department(s). Integrates subject matter and industry expertise within a defined area. Contributes to standards around which others will operate. Requires in\-depth understanding of how areas collectively integrate within the sub\-function as well as coordinate and contribute to the objectives of the entire function. Requires basic commercial awareness. Developed communication and diplomacy skills are required in order to guide, influence and convince others, in particular colleagues in other areas and occasional external customers. Has responsibility for volume, quality, timeliness and delivery of end results of an area. May have responsibility for planning, budgeting and policy formulation within area of expertise. Involved in short\-term planning resource planning.Full management responsibility of a team, which may include management of people, budget and planning, to include duties such as performance evaluation, compensation, hiring, disciplinary and terminations and may include budget approval. **Responsibilities:** * Develops, enhances, and validates the methods of measuring and analyzing risk, for all risk types including market, credit and operational. Also, may develop, validate and strategize uses of scoring models and scoring model related policies. * Manages model risk across the model life\-cycle including model validation, ongoing performance evaluation and annual model reviews. * Produces analytics and reporting used to manage risk for Citi's operations. * Translates operational requests from the business into programming and data criteria and conduct systems and operational research in order to model expected results. * Assists in the development of analytic engines for business product lines. * Communicates results to diverse audiences. * Conducts analysis and packages it into detailed technical documentation report for validation purposes sufficient to meet regulatory guidelines and exceed industry standards. * Participates on teams to solve business problems. * Identifies modeling opportunities that yield measurable business results. * Provides guidance to junior validators as and when necessary. * Manages stakeholder interaction with model developers and business owners during the model life\-cycle. * Represents the bank in interactions with regulatory agencies, as required. * Presents model validation findings to senior management and supervisory authorities. * Provides effective challenge to model assumptions, mathematical formulation, and implementation. * Assesses and quantifies model risk due to model limitations to inform stakeholders of their risk profile and development of compensating controls. * Contributes to strategic, cross\-functional initiatives within the model risk organization. * Full management responsibility of a team, which may include management of people, budget and planning, to include duties such as performance evaluation, compensation, hiring, disciplinary and terminations and may include budget approval. * Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency, as well as effectively supervise the activity of others and create accountability with those who fail to maintain these standards. **Qualifications:** * 6\-10 years experience * Consistently demonstrates clear and concise written and verbal communication skills * Self\-motivated and detail oriented * Demonstrated project management and organizational skills and capability to handle multiple projects at one time . * Practical experience using SAS or similar statistical coding software to build and test prediction models. comfortable interfacing with business clients. proficiency handling very large data sets. * Experience in a quantitative role in risk management at a financial institution with experience in either model development or validation. * Good knowledge and understanding of a variety of model development and validation testing techniques covering risk models. **Education:** * Bachelor’s/University degree or equivalent experience, potentially Masters degree **Job description** * Ensure that models in use have undergone appropriate validation and approval processes, promptly identify new or changed models, and provide all necessary information for validation activities. * Collaborate with Model Developers in the development of new scoring models as per business requirement. This position will be exposed to different areas of Credit Risk team and several modeling approaches * Develop ad\-hoc analysis to understand the performance of the models according with the Risk managers needs. * Appropriately applying the model governance policy and the documentation requirements defined by Model Risk Management Policy * Interaction with internal and external audit reviews related with risk models * Track and execute corrective action plans due to audit review observations in proper time * Ongoing management and validation of risk decision models across portfolios * Effective interaction with risk managers, risk infrastructure and business areas **Knowledge and Experience** * BS in an analytics\-related field, such as data science, Mathematics, Actuarial Science, Engineering, Operations Research, or related fields * Master’s degree is a plus. * 8\+ years experience in analytical areas related to risk management * Understanding of consumer risk management preferred * Coding experience to include SAS, SQL, Python or R * Must speak and write English proficiently * Experience coordinating analytical teams **Skills and competencies** * Solid knowledge and understanding of modeling concepts * Excellent organizational, attention to detail and ability to complete assignments in a timely manner * Demonstrated analytic and problem solving skills * Excellent written and verbal communication skills, and be able to prepare presentations for senior managers * Ability to summarize and communicate results from complex analysis \- **Job Family Group:** Risk Management \- **Job Family:** Model Development and Analytics \- **Time Type:** Full time \- **Most Relevant Skills** Analytical Thinking, Business Acumen, Constructive Debate, Data Analysis, Escalation Management, Policy and Procedure, Policy and Regulation, Risk Controls and Monitors, Risk Identification and Assessment, Statistics. \- **Other Relevant Skills** For complementary skills, please see above and/or contact the recruiter. \- *Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law.* *If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review* *Accessibility at Citi**.* *View Citi’s* *EEO Policy Statement* *and the* *Know Your Rights* *poster.*

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Legal Specialist (NDAs & Ancillary Documents)65110045172609124

Legal Specialist (NDAs & Ancillary Documents)

Join **Scissero** – The Law Firm of the Future **About Us** Scissero is an AI\-enhanced legal services company built for financial institutions. We combine expert legal support with intelligent automation, transforming how transactional law is delivered. We’re not a traditional law firm. We are a diverse and globally distributed team of lawyers, engineers, and innovators working across the U.S, EMEA, and APAC. We believe technology augments, not replaces legal expertise. Our culture values collaboration, inclusivity, and flexibility. **Position Overview / Summary of the Role:** As a **Legal Specialist**, you will gain hands\-on experience drafting, reviewing, and negotiating contracts for global clients across a range of sectors, working right at the heart of our legal tech model. This is a chance to take a less traditional route in legal services, combining practical legal work with deep exposure to AI\-driven tools and workflows, while building technical expertise alongside your existing legal knowledge and skill set. **Key Responsibilities** * AI\-Assisted Review: Use Scissero’s AI tools to perform rapid, high\-accuracy reviews of NDAs, back\-to\-backs (B2Bs), non\-reliance letters (NRLs) and other ancillary documents. * Playbook Application: Review contracts against client\-approved playbooks, identify deviations from agreed positions, and apply the appropriate standard or fallback language in line with client guidance. * Quality \& Precision: Maintain a "zero\-error" mindset, ensuring that all mark\-ups are consistent, professional, and delivered within tight turnaround times (SLAs). * Workflow Coordination: Own and manage your own queue of documents, balance volume and urgency to ensure efficient, timely delivery for our global clients. * Tech Feedback: Regularly report to our product teams on how the AI is performing, helping us "train" the models to be even more accurate. **Skills and Qualifications Required:** * Degree in Law or a similar legal qualification. * 1–3 years of experience in a high\-volume, process\-oriented environment (gained at law firms, corporate legal departments, or within compliance or contract administration). * Ideally, you will have experience drafting, reviewing, and negotiating transactional documents for clients in the private equity and alternative asset space (including NDAs, B2Bs and NRLs), and be familiar with US/common law contract structures and terminology. * Advanced English (written and spoken) is mandatory for daily collaboration with US\-based clients and stakeholders. **Why Join Us?** * Gain valuable experience at the forefront of AI\-enhanced legal services. * Work with a diverse and innovative global client base, including leading financial institutions. * Opportunity for professional growth and development in a tech\-enabled environment. * Join a dynamic, enthusiastic, and diverse team committed to collaboration and excellence. * Learn from experienced professionals across multiple disciplines and jurisdictions. **Global Benefits** * Hybrid and remote working options, with the ability to work from other countries (upon request) * Paid Sick Leave: 7 days per year to recover or care for family. * Confidential Support: Employee Assistance Programme (EAP) offering mental health and wellbeing support. * Professional Development: 7 days per year of paid study leave annually for exams and structured learning. * Annual Bonus: Discretionary and performance\-based. * Generous Paid Time Off: 25 days annual leave. At Scissero, you’ll be part of a scale\-up blending law and technology to create meaningful impact. If you’re excited about redefining the future of legal services with AI, apply now to join our team. **Inclusivity** At Scissero, we value diversity in all its forms and believe that varied perspectives make us stronger. We welcome applications from candidates of all backgrounds, identities, and experiences and are committed to creating an inclusive environment where everyone can thrive.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Field Engineer65109686310785125

Due to expansion, a company specializing in **ATMs** is seeking a Field Engineer. Responsibilities: \* Diagnosis and Resolution \* On-site customer support \* Installation and Maintenance \* Documentation: Create and maintain detailed records of incidents (tickets) and solutions (manuals). \* Follow-up. \* Time management and punctuality \* Must possess and demonstrate 100% availability for field work. Soft Skills: \* Clear and empathetic communication (**with non-technical users**). \* Active listening and problem analysis. \* Time management \* Sense of urgency \* Customer service orientation We offer: \* Competitive salary based on experience \* Statutory benefits \* Bonuses (after probation period) \* Opportunities for professional development within the company Job type: Full-time Salary: $11,000.00 \- $13,000.00 per month Benefits: * Free uniforms Willingness to travel: * 25 % (Desirable) Work location: On-site employment

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 11,000-13,000/year

Recent Graduates in Computer Systems, Computing, or Information Technology65109686279043126

Recent Graduates in Computer Systems, Computing, or Information Technology

**Description** Digis01 Digital Solutions is a company characterized by a team of young, highly skilled technology professionals. This growth stems from the strong commitment of our employees, who dedicate themselves to delivering an innovative approach to our clients—combining deep technical knowledge with extensive experience in software consulting and application development. We are seeking recent graduates in Computer Systems or Information Technology who have enthusiasm and passion for programming. **Requirements:** * Responsible, Proactive * Passionate about technology **Responsibilities:** * Analysis and design of systems for technology projects. * Collaboration in application development using Microsoft .NET or Java technologies. * Participation in the full application development lifecycle for web applications—from requirements gathering through implementation and testing. * Identification and resolution of technical issues, ensuring optimal system performance. **Benefits:** * Salary: 8\.000\-10\.000 per month * Opportunity for professional growth. **Work Location:** * Avenida Paseo de la Reforma, Col. Cuauhtémoc, Mexico City * Across from Reforma 222 and a few blocks from Metrobús Reforma or Hamburgo stations. If you are interested and meet the position requirements, apply through this channel so we can contact you. Job Type: Full-time, Indefinite-term Salary: $8,500\.00 \- $10,000\.00 per month Application Question(s): * What is your age? * What was your university GPA? Workplace: On-site employment

Guanajuato 54, Roma Nte., Cuauhtémoc, 06700 Ciudad de México, CDMX, Mexico

$MXN 8,500-10,000/month

SAP Employee Central Payroll Consultant – Project-Based65109686232194127

SAP Employee Central Payroll Consultant – Project-Based

We are seeking a highly specialized SAP Employee Central Payroll Consultant to participate in the implementation, optimization, and support of the payroll solution within the SAP SuccessFactors environment. You will be responsible for ensuring seamless integration between Employee Central (EC) and Payroll, guaranteeing legal compliance and efficiency in compensation processes. **Key Responsibilities:** * Participate in the analysis, design, configuration, and testing of the SAP Employee Central Payroll module. * Collaborate with functional and technical teams to ensure proper integration among modules and associated systems (EC, HR, Finance, etc.). * Conduct requirements gathering with the client and produce corresponding functional documentation. * Execute unit, integration, and user acceptance testing (UAT). * Resolve payroll-related incidents and technical issues. * Provide training or knowledge transfer to the client’s internal team. * Ensure compliance with applicable legal and tax regulations related to payroll. * Propose improvements and optimizations to payroll management processes. **Requirements:** * Bachelor’s degree in Computer Science, Engineering, Human Resources, or related fields. * Minimum 3–5 years of experience in SAP projects, preferably in SuccessFactors Employee Central Payroll. * Solid understanding of payroll processes and labor legislation in the country of operation. * Experience with SAP EC–ECP integrations (Point-to-Point, APIs, etc.). * Strong analytical and problem-solving skills. **Desired Competencies:** * Results-oriented with strong time-management and deadline adherence. * Collaborative teamwork and effective communication. * Adaptability to change in project environments. * Ability to document and implement best practices. Employment Type: Full-time, Project-based or Fixed-term Contract Duration: 6 months Salary: $50,000.00 – $55,000.00 per month Benefits: * Grocery vouchers Application Question(s): * Are you agreeable to this position being a 6-month project? Experience: * SAP configuration: 2 years (Mandatory) Work Location: Remote/hybrid in 03230, Actipan, CDMX

Av. Insurgentes Sur 1464, Actipan, Benito Juárez, 03230 Ciudad de México, CDMX, Mexico

$MXN 50,000-55,000/year

Warehouse Assistant65109686185729128

Warehouse Assistant

**GRUPO MAYA PROTECCIÓN PERSONAL PRIVADA Y EMPRESARIAL SA DE CV is seeking a Warehouse Assistant in Del Valle - Benito Juárez, Mexico City** ------------------------------------------------------------------------------------------------------------------------------------------- **Position Objective** Ensure the proper receipt, storage, safeguarding, preparation, and dispatch of goods in the warehouse, maintaining shipment integrity and contributing to efficient logistics operations. **Key Responsibilities:** * Posting and Promotion: Post job openings on various channels (job boards, social media, Facebook groups) * Initial Interviews: Conduct telephone, in-person, or virtual interviews to assess basic competencies. * Assessments: Administer and grade psychometric, knowledge-based, or technical tests as required by the role profile. * File Management: Request and validate documentation from selected candidates to ensure complete files prior to hiring. * Process Follow-up: Contract signing and onboarding. * Indicator Reporting: Maintain updated KPIs (time-to-fill, most effective recruitment sources, early turnover rate). **Position Objective** Attract, screen, and select candidates quickly and efficiently to fill high-volume operational vacancies. **Key Responsibilities:** * Receive, inspect, and register incoming packages according to established procedures. * Store goods in designated areas, respecting order and storage conditions. * Prepare orders for shipment, ensuring correct classification and packaging. * Scan packages for system control and tracking. * Conduct periodic physical inventory counts and report any incidents or anomalies. * Assist with warehouse cleaning, organization, and maintenance. * Comply with safety regulations and internal procedures. * Report damage, shortages, or issues detected in goods or work equipment. **We Offer:** * Schedule: Monday to Friday, 9:00 am to 6:00 pm; Saturday, 9:00 am to 2:00 pm. * Statutory benefits. * Savings fund. * Life insurance. * Monthly net salary of $9,000 plus a $2,000 bonus based on KPIs. **Profile Requirements:** * Education: Completed high school diploma. * Experience: 1–2 years as a warehouse assistant. * Proficiency in software for inventory intake and dispatch. * Experience handling large volumes of merchandise. **Desired Education Level:** Upper Secondary **Desired Experience Level:** Expert Level **Departmental Function:** Commercial / Sales **Industry:** Warehousing and Storage *This vacancy originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j_id=696a83f445000031006ae607&source=indeed*

Manuel López Cotilla 856, Col del Valle Centro, Benito Juárez, 03100 Ciudad de México, CDMX, Mexico

$MXN 9,000/month

Inspector de Calidad65109686169986129

Inspector de Calidad

**¡CONTRATACIÓN INMEDIATA Y PRESTACIONES DESDE EL PRIMER DÍA!** Empresa en el sector de fabricación de envases. **VACANTE: INSPECTOR DE CALIDAD** Experiencia y conocimientos: Experiencia mínima de **1 año** en el puesto. Escolaridad: Técnico / Preparatoria Actividades: * Realizar las mediciones y pruebas relacionadas con la calidad del producto. * Registrar en el software los resultados obtenidos en las mediciones de calidad del producto. * Realizar las entradas e inspecciones de calidad en materias primas y materiales indirectos de fabricación. * Apoyar en la inspección de calidad de la botella PET. * Realizar la certificación de calidad del producto para embarque. * Etiquetado del producto conforme y no conforme, tanto en la recepción de materiales como durante el proceso. * Realización de auditorías internas. * Mantener las áreas de trabajo limpias y ordenadas. * Mantener las áreas de trabajo limpias y ordenadas. * Inspeccionar la limpieza del personal, áreas, equipos y utensilios utilizados durante la fabricación del producto. * Verificar que, durante el proceso, el personal tenga disponibles las instrucciones correspondientes y registre adecuadamente los datos pertinentes. **OFRECE**: * Contratación directa, * prestaciones superiores a las establecidas por la ley, * salario base, * caja de ahorro, * uniformes, * equipo de protección. Preferentemente: Personas que residan en Cuautitlán Izcalli, Estado de México, o en zonas cercanas. Interesados **POSTÚLENSE POR ESTE MEDIO Y NOS PONDREMOS EN CONTACTO.** Tipo de puesto: Tiempo completo Sueldo: $15,300.00 al mes Beneficios: * Caja de ahorro * Opción a contrato indefinido * Uniformes gratuitos Lugar de trabajo: Empleo presencial

C. Lázaro Cárdenas 66, San Francisco Tepojaco, 54745 Cuautitlán Izcalli, Méx., Mexico

$MXN 15,300/year

Accountant651096860750111210

**Description** Ensure proper and transparent financial management of the organization, guaranteeing compliance with Mexican tax and accounting regulations—particularly those applicable to organizations with authorized donee status. This includes efficient resource management, timely and clear presentation of financial reports, accurate determination and payment of taxes, as well as administration of accounting and resources allocated to the organization’s social objectives. Additionally, transparency in fund usage must be maintained, ensuring auditability of processes and compliance with legal requirements to preserve authorized donee status. This position also plays a key role in the organization’s collective work, facilitating financially sound decision-making that supports the organization’s goals, always from a human rights perspective. Likewise, the accountant will continuously collaborate with the Aluna team, ensuring ethical resource management in alignment with institutional principles and policies, for the benefit of the community. **Profile/Requirements** * **Bachelor’s degree in Accounting, with work experience in civil society organizations in Mexico.** * Experience with tax obligations required of an authorized donee. * Experience in audit processes. * Proficiency in Contpaqi accounting software.\* * Ability to analyze laws and regulations governing accounting and administrative processes. * Capacity to understand diverse types of accounting information. * Proficiency in basic computer software, Excel, and accounting programs and tools. * **Submit your CV and a letter of intent (maximum one page).** * **Provide two references who may be contacted (include contact details).** ***Working Conditions:*** * On-site work, with possibility of hybrid arrangements. * Statutory benefits. * Vacation period exceeding the statutory minimum. * Three-month probationary period. **Competencies:** Problem analysis and resolution, Initiative and autonomy, Learning capacity, Organization and planning, Technical and personal reliability, Teamwork, Transparency **Level:** Employee **Contract type:** Full-time **Duration:** Indefinite **Salary:** Between $22,001.00 and $25,000.00 pesos gross/month **Minimum education:** Bachelor’s degree **Minimum experience:** At least 3 years **Start date:** 09/02/2026 **Number of vacancies:** 1

Manuel López Cotilla 856, Col del Valle Centro, Benito Juárez, 03100 Ciudad de México, CDMX, Mexico

$MXN 22,001-25,000/year

Software Designer651096860108811211

Software Designer

Are you looking for a great job opportunity? Come and join us as a Software Designer Benefits you will enjoy with us: * + Competitive salary according to experience. + Statutory benefits + Professional development opportunity. + Growth opportunity + Positive work environment. **What do you need to apply?** * + Bachelor's degree in Systems Engineering, Information Technologies or related fields. + Minimum 6 months of experience in software design, development and analysis. + Advanced knowledge of programming languages such as Java, Python, C\+\+ or similar. + Experience with databases (SQL, NoSQL). + Knowledge of agile methodologies and project management tools (Scrum, Jira, etc.). + Ability to identify and resolve technical issues. + Analytical skills and attention to detail. **Responsibilities** * + Design and develop custom software applications and systems according to company needs. + Perform requirements analysis and design appropriate technical solutions. + Conduct testing to ensure correct software functionality and quality. + Collaborate with cross-functional teams to define, develop and implement software solutions. + Maintain existing systems and perform continuous improvements. * Integration of tenders (SEDENA, SEMAR, IMSS and ISSSTE) **Schedule:** * Monday to Friday from 9:00 to 18:00 hrs, with a 1-hour lunch break. * Saturday from 9:00 to 14:00 hrs.

Monte Casino 100, Molino del Rey, Miguel Hidalgo, 11100 Ciudad de México, CDMX, Mexico

Recruitment Assistant651096859778571212

Recruitment Assistant

Position Objective: Support the Human Resources department in recruitment and selection processes, ensuring an efficient and timely search for talent through the use of digital platforms, social media, and optimization of hiring processes. Main Responsibilities: * Post job openings on employment portals: Computrabajo, OCC, Indeed, Pandapé, LinkedIn. * Promote job opportunities on social media: LinkedIn, Facebook. * Efficiently screen and select resumes (CVs). * Coordinate interviews and candidate follow-up. * Administer psychometric tests and prepare results reports. * Maintain updated candidate databases and recruitment reports. * Support headhunting strategies and talent attraction initiatives. **Requirements:** * Bachelor’s degree in Psychology, Human Resources, Administration, Technical Career, or related field. * Minimum 6 months’ experience in personnel recruitment and selection (preferred). * Knowledge of recruitment platforms, social media, and online job boards. * Basic proficiency in Microsoft Office suite. * Excellent writing, spelling, and communication skills. * Proactive, organized, and results-oriented. **Competencies and Skills:** * Planning and organization of processes. * Teamwork and collaboration. * Ability to learn quickly. * Results-focused with commitment to goal achievement. We Offer: * Competitive salary and statutory benefits. * Excellent work environment. **Schedule: Monday to Friday from 09:00 to 18:00 hrs (including one hour for lunch); Saturday from 09:00 to 14:00 hrs.**

Monte Casino 100, Molino del Rey, Miguel Hidalgo, 11100 Ciudad de México, CDMX, Mexico

sub chef651096859293471213

Hospital Ángeles Lindavista We are seeking a **Sub\-chef** Requirements: * Education: Bachelor’s degree with 100% credits completed * Experience: Staff management, preparation of all types of food. (Technical test required) * Shift: Flexible availability We offer: * Salary: $13,665\.00 gross monthly * Complimentary uniform * Benefits exceeding statutory requirements * Savings fund * Grocery vouchers: $1,200\.00 monthly * Training, etc. **Please bring:** * Resume or job application form * Official ID (INE) (required for entry) If you meet the profile, please attend our **MASS RECRUITMENT** on the 19th, 20th, 21st, 22nd, 23rd, and 26th of this month, from 9:00 to 11:00 a.m. Address: Rio Bamba Street #639, Magdalena de las Salinas neighborhood, ZIP Code 07760\. (Entrance is on Rio Bamba Street) Landmark: We are located across from Plaza Parque Lindavista Position type: Indefinite-term employment Salary: $13,665\.00 per month Benefits: * Eligibility for indefinite-term contract * Free uniforms * Grocery vouchers Experience: * Culinary experience: 1 year (preferred) Work location: On-site employment

Benito Juárez 12, Magdalena de las Salinas, Gustavo A. Madero, 07760 Ciudad de México, CDMX, Mexico

$MXN 13,665/year

Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)650957561669151214

Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104568 Not ready to apply? Join our Talent Network **Description** Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** JOB SUMMARY The IMS Budget Specialist I plays an important role to the Clinical Development Services team. As the liaison between Operations Management, Site Contracts, Clinical Operations, Investigator Management Solutions Payments Team, the IMS Budget Specialist I will provide analytical insight and support reviewing site budgets, study protocols, and ensuring alignment within the dedicated clinical trial management system. JOB RESPONSIBILITIES  Analyzes and interprets the payment terms and conditions of fully executed site clinical trial agreement (CTA).  Ensures accuracy of contract budget \& clinical trial management system (CTMS) template alignment.  Inputs site budget cost utilizing the templates within CTMS.  Engages project team with the quality control of the cost structure created within CTMS.  Serves as subject matter expert for department and project teams concerning contract interpretation and development of payment strategy.  Ensures the presence of required vendor financial account details participating in clinical trial.  Ensures acquisition and completeness of tax related documentation.  Participates in payment setup issue resolution.  Liaises with internal departments including the Operations, Finance, and Legal teams.  Performs a variety of administrative functions, updates and maintains setup details and progress status of contractual site budgets in the database, and other related duties as assigned.  Works with enterprise financial systems.  Ability to multi\-task on several projects. Possess strong communication skills and be an effective team player.  Proactively participates in Investigator Payment Planning (IPP) Meetings, providing input to payment strategy planning for incoming studies.  Minimal travel may be required (up to 25%). QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’)  Bachelor’s degree, or equivalent education and experience, plus minimal experience in contract administration or finance.  Requires strong communication, verbal, written, and interpersonal.  Ability to build team relationships with line management, employees, and HR team.  Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail.  Ability to interact and build relationships with all levels of employees.  Ability to organize and prioritize work to meet frequent deadlines is essential.  Strong customer services skills and ability to maintain confidentiality. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Mgr, FSP 360650957561509141215

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104647 Not ready to apply? Join our Talent Network **Description** Mgr, FSP 360 Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Overall, the role will be responsible for three primary performance areas:** **1\) Customer Delivery and Success** * Develops and fosters strong, collaborative relationships with customers. Solicits feedback from customer PoC (s) for continuous improvement of service delivery and to strengthen customer relationships on an individual or (PoC) country\-specific level. * Responsible for delivery and compliance with agreed\-upon KPIs in relation to daily activities of their team members; develops and executes mitigation and remediation plans for non\-compliance as needed. * Responsible for headcount management, in relation to their own team, to ensure resource needs are identified and addressed in a timely fashion. Responsible for creation of job requisitions at expected level of quality. * Proactively communicates and manages customer issues through assigned escalation channels. * Ensures quality and adherence to Standard Operating Procedures/Work Instructions (SOP/WIs) and compliance with federal and local guidelines and ICH GCPs. Ensures all staff follow the required training and complete the required documentation. Provides regular compliance updates to management accordingly. * Conducts oversight visits as required for Clinical Research Associates. * Responsible for all system updates, and compliance with systems and relevant procedure and practices applicable to the customer and Syneos Health processes. **2\) Business Impact** * Responsible for knowledge sharing across their own team to disseminate best practices and lessons learned in support of the overall FSP 360 operating model. Makes informed and data\-driven decisions that positively impact their own team's performance within the business unit. * Responsible for delivering BU revenue targets by attracting and retaining the right talent. Responsible for balancing the right size and skill level team against the expected customer delivery. * May serve as a Company representative at professional meetings or seminars. 3\) **People Leadership** * Responsible for active management of team members’ performance through the established Syneos Health process; at an individual contributor level. * Verifies that team members adhere to training guidelines, maintain their training records and individual and corporate training needs are identified and addressed. * Provides administrative oversight (for example, HR processes, timecards, expense reports). * Supports team members’ professional development through coaching, providing opportunities to increase knowledge and skill levels, and by delegating tasks commensurate with skill level. * Proactively works to ensure team members’ engagement, retention and turnover rates remain within expected levels. * Demonstrates commitment to diversity, equity, and inclusion through continuous development of all staff, modeling inclusive behaviors and proactively managing bias. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for interacting and engaging with internal and external stakeholders for functional team members, acting as a Syneos Health ambassador with customers. Responsible for managing team members’ performance in line with project deliverables. Accountable for direct supervision of FSP 360 multifunctional staff. May act as an SME where country/region/functional knowledge is key.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist I or II (CPQA & medical devices experience) Home Based Mexico650957561349151216

Safety & PV Specialist I or II (CPQA & medical devices experience) Home Based Mexico

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104865 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist I or II (CPQA \& medical devices experience) Home Based Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. * Fosters constructive and professional working relationships with all project team members, internal and external. * Participates in audits as required/appropriate. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Qualifications: * Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job. * Safety Database systems and knowledge of medical terminology required. * Good understanding of clinical trial process across Phases II\-IV and/or post\-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance. * Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet. * Ability to work independently and in a team environment. * Excellent communication and interpersonal skills, both written and spoken. * Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. * Detail oriented with a high degree of accuracy and ability to meet deadlines. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Pharmacovigilance \& Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial\-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist (case processing) Hybrid Mexico650957561182741217

Safety & PV Specialist (case processing) Hybrid Mexico

**Updated:** December 4, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25103060 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist (case processing) Hybrid Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. * Fosters constructive and professional working relationships with all project team members, internal and external. * Participates in audits as required/appropriate. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Qualifications: * Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job. * Safety Database systems and knowledge of medical terminology required. * Good understanding of clinical trial process across Phases II\-IV and/or post\-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance. * Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet. * Ability to work independently and in a team environment. * Excellent communication and interpersonal skills, both written and spoken. * Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. * Detail oriented with a high degree of accuracy and ability to meet deadlines. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Pharmacovigilance \& Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial\-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Sr Clinical Data Scientist CDM (Hybrid -ARG & MEX Only)650957561017631218

Sr Clinical Data Scientist CDM (Hybrid -ARG & MEX Only)

**Updated:** December 16, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102142\-OTHLOC\-7304\-2DH Not ready to apply? Join our Talent Network **Description** Sr Clinical Data Scientist CDM (Hybrid \-ARG \& MEX Only) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** \*\*\*This role is only open to hiring in Argentina and Mexico. Hybrid \- 2 days in office per week (Buenos Aires and Mexico City) \*\*\*Proficiency in English is required \- Please submit CVs in English. \*\*\*Previous experience within Veeva Vault is required. * Serves as Functional Lead for Clinical Data Science including primary contact for internal liaison between Clinical Data Science and Project Management, Clinical Monitoring, and other functional groups* Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross functional operational plans to drive comprehensive clinical data quality* Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined study analysis* Works with assigned project teams to communicate, address, troubleshoot and resolve data related questions and recommends potential solutions; escalates issues which potentially impact patient safety and study analysis* Coordinates cross functional data cleaning activities to ensure quality standards and timelines are met for clinical data deliverables Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined project analysis* Drives the development of the clinical data acquisition plan and corresponding data flow diagram with the study team, assess risks associated with protocol design, study set parameters that could impact the credibility and reliability of the trial results, aligns data flow with the study protocol to ensure data collected meets regulatory and study endpoint requirements.* Drives the development of analytical tools, utilizes analytical platform/dashboard to detect potentially unreliable data that may impact the validity of the trial results Performs analytic reviews as defined in scope of work and data acquisition plan, identifies root cause to systematically resolve data issues* Monitors and communicates project progress to the Sponsor and project team including use of project status reports and tracking tools/metrics* Ensures launch, delivery and completion of all Clinical Data Sciences activities and milestones according to contractual agreement and relevant Standard Operating Procedures (SOPs), guidelines, and regulations* Review, maintain budget and identify out of scope for Clinical Sciences activities, raise to PM to be implemented in required change order* Plans, manages, and requests Clinical Data Science resources for assigned projects* Coordinates the work of the assigned Clinical Data Science team* Develops and maintains project plans, specifications, and documentation in line with SOP requirements* Maintains documentation on an ongoing basis and ensures that all TMF filing is up to date for necessary files* Participates in, and presents at internal, Sponsor, third\-party, and investigator meetings on behalf of clinical data science responsibilities* Prepares input, and participates in proposal bid defense meetings and request for proposals on behalf of clinical data science responsibilities* Plans for and creates necessary documentation to support internal and external audits; participates in such audits on behalf of clinical data sciences responsibilities* Trains and mentors new or junior team members* Maintains proficiency in Clinical Data Science systems and processes through regular training. May attend/represent the company at professional meetings/conferences* Performs other work\-related duties as assigned. Minimal travel may be required (up to 25%)**Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for the end\-to\-end coordination of cross functional data collection and cleaning activities to ensure clinical study data deliverables are fit for purpose and align with the executed contract and sponsor expectations and timelines.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

CSR Appendices Coordinator - RIMS System Exp preferred650957560857621219

CSR Appendices Coordinator - RIMS System Exp preferred

**Updated:** January 10, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25103128\-OTHLOC\-7302\-2DR Not ready to apply? Join our Talent Network **Description** CSR Appendices Coordinator \- RIMS System Exp preferred Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Roles and Responsibilities:** * Defines scope of Clinical Study Reports (CSR) Appendices with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS). * Confirm completeness of documents (e.g. Casebooks, Literature References) by obtaining, compiling, and organizing in the regulatory information management system (RIMS). Maintain strong knowledge of CSR and CSR Appendices and CTD structure. * Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills. * Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for authoring of Clinical Study Report (CSR) Appendices and managing clinical and regulatory references.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist II - MXN Office Based - Exp in Mailbox Mgmt & All Report Processing would be preferred.650957560695051220

Safety & PV Specialist II - MXN Office Based - Exp in Mailbox Mgmt & All Report Processing would be preferred.

**Updated:** December 3, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102866 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist II \- MXN Office Based \- Exp in Mailbox Mgmt \& All Report Processing would be preferred. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** Job Description* Enters information into PVG quality and tracking systems for receipt and tracking ICSR as required. * May assist in the preparation of the project plans such as Safety Management Plan. * May perform set\-up, delivery and close\-out of safety and pharmacovigilance projects. * Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans. * Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. * Enters data into safety database. * Codes events, medical history, concomitant medications, and tests. * Compiles complete narrative summaries. * Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved. * Participates in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, and MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Quality review for the work performed by peers. * Serves as a subject matter expert in SPVG, which includes resolution of project related routine queries; mentoring, coaching, and training of new hires. * Fosters constructive and professional working relationships with all project team members, internal and external. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. * Ensures distribution of all required individual expedited and periodic reports for both clinical and post\-marketing projects to the Safety Submissions team if contracted to submit the reports. * Participate in audits/inspections as required. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Job Description Summary Performs safety and pharmacovigilance program delivery activities including (but not limited to) all aspects of the collection, processing, and reporting of individual cases safety reports (ICSRs), literature screening and review for safety, drug coding, maintenance of drug dictionary, Medical Dictionary for Regulatory Activities (MedDRA) coding, data management activities which includes cleaning and validation of data (xEVMPD product dictionary, manual recoding of substance/product terms arising from ISCR reports, management of duplicate ICSR cases, Quality review of ICSRs, Substances, Products, Organizations and Referential (SPOR) / Identification of Medicinal Products (IDMP) activities)) and the preparation of expedited and periodic safety reports, while adhering to all data privacy guidelines, Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program\-specific procedures for clinical trials and/or post\-marketing safety programs. The processing of information may include filtering, cleaning, migrating, analyzing, reporting, filing or publication of data and information.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

CRA II or Sr CRA assign to client CDMX Mexico650957560531221221

CRA II or Sr CRA assign to client CDMX Mexico

**Updated:** January 6, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25101362 Not ready to apply? Join our Talent Network **Description** CRA II or Sr CRA assign to client CDMX Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Conduct on\-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms * Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates * Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials * Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues * Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow\-up letters, and action plans * Collaborate with cross\-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct **Qualifications:** * Bachelor's degree in a related field or equivalent experience * Minimum of 2\-4 years of experience in clinical research monitoring * Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements * Excellent communication and interpersonal skills * Ability to work independently and manage multiple priorities * Proficiency in using clinical trial management systems and other relevant software **Certifications:** * Certified Clinical Research Associate (CCRA) or equivalent certification preferred **Necessary Skills:** * Attention to detail and strong analytical skills * Problem\-solving abilities and critical thinking * Ability to work effectively in a team environment * Strong organizational and time management skills * Proficiency in Microsoft Office Suite *We are always excited to connect with great talent. This posting is intended for an* *upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.* We are always excited to connect with great talent. This posting is intended for a \[possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on\-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Impact and Contribution Roles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes. Core Focus • Conduct thorough on\-site and remote monitoring of clinical research studies • Develop and implement tools, procedures, and processes to ensure quality monitoring • Manage defined components of projects or processes within their area of responsibility • Utilize practical knowledge of a professional area, typically obtained through education combined with experience • Maintain high standards of clinical practice and ensure the success of clinical trials

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Medical Editor II - (Formatting Regulatory Documents) - Home Based650957560366111222

Medical Editor II - (Formatting Regulatory Documents) - Home Based

**Updated:** January 6, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102337\-OTHLOC\-7302\-2DR Not ready to apply? Join our Talent Network **Description** Medical Editor II \- (Formatting Regulatory Documents) \- Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Roles and Responsibilities:** * Defines scope of formatting of clinical and regulatory documents with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS). * Ensure document format and styles are consistent with the defined in RIMS and are consistent with the clinical and regulatory templates. Ensure document properties and naming conventions are used. Maintain strong knowledge of RIMS styes and formatting standards. * Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills. * Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for ensuring the quality of clinical and regulatory documents are formatted to the requirements in the AbbVie style guide and document templates.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Support Specialist, Technical650957558949131223

Support Specialist, Technical

The Support Specialist, Technical is responsible for providing advanced technical support to Restaurant365 customers across the R365 platform. This role focuses on troubleshooting configuration, workflow, and data\-related issues in a complex SaaS / ERP environment, supporting business critical restaurant operations. The ideal candidate brings strong technical aptitude, structured problem\-solving skills, and the ability to communicate clearly with both technical and non\-technical stakeholders. ### **How you'll add value:** * Provide technical support for Restaurant365 platform * Manage customer communications through tickets, live chat, and outbound phone support * Gather detailed technical and business information from customers to troubleshoot reported issues * Diagnose configuration, workflow, and data\-related issues and deliver accurate solutions * Educate customers on Restaurant365 system functionality and best practices * Route non\-technical or non\-applicable issues to appropriate teams when necessary * Identify, document, and escalate suspected software defects with clear reproduction steps and impact details * Participate in live chat rotations * Manage a personal queue of customer tickets while meeting SLA and quality standards * Identify gaps in internal and customer\-facing documentation and contribute improvements * Assist Support leadership in rolling out new platform features or workflows * Demonstrate reliable and punctual attendance across assigned shifts, including remote or hybrid setups, while ensuring clear and timely communication with management regarding availability, scheduling changes, or unforeseen delays — particularly when supporting customers across multiple time zones ### **What you'll need to be successful in this role:** * High attention to detail, particularly when working with system configuration and financial data * Strong Excel skills, including data review and validation * Flexible and adaptable to shifting customer and team needs * Solution\-oriented mindset with the ability to troubleshoot and communicate clearly under pressure * Excellent written and verbal communication skills, with the ability to simplify complex technical concepts * Strong technical aptitude and comfort working across multiple support platforms (ticketing systems, chat, outbound phone) * Experience working with integrated systems and understanding how data flows between applications * Reliable and punctual attendance in assigned shifts and workdays including providing clear and timely communication with management regarding availability and scheduling changes **PREFERRED QUALIFICATIONS*** Bachelor’s degree with emphasis in business, finance, accounting, or information systems * Restaurant industry experience * Strong understanding of general business processes and workflows * Previous experience in a technical support or customer\-facing technical role * Experience supporting SaaS or ERP platforms (e.g., enterprise software, financial systems, or operational management tools)

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

CCTV INSTALLATION TECHNICIAN650956419873291224

CCTV INSTALLATION TECHNICIAN

Join us as a **CCTV Installation Technician**! We are a company committed to excellence in service and the well-being of our workforce. **Requirements** * Minimum education level: high school or equivalent (technical training preferred). * Experience installing CCTV, access control systems, and electronic security systems. * Knowledge of CAT cable termination. * Proficiency with tools (drill, cable punch-down tool, tester, etc.). * Cable laying and routing (UTP, coaxial, and power cables). * Assistance with work at heights. * Preferred: basic knowledge of electricity, electronics, or networking. * Experience installing and maintaining CCTV equipment. * Willingness to learn and follow established procedures. * Responsible, punctual, and service-oriented. * Ability to work effectively in a team. * Desire for professional development and growth. **Main Responsibilities** * Installation and basic support of security cameras (CCTV). * Support in data network and structured cabling installations. * Basic installation of IP telephony, access control, and alarm systems. * Conduit installation, cable laying, and termination (UTP, raceways, and conduits). * Support in preventive and corrective maintenance. * On-site work at client locations. * Basic completion of service reports and assistance to the lead technician. **We Offer** * Salary: **$11,000 net monthly** * Statutory benefits * Growth opportunities * Schedule: * Monday to Friday, **09:00 to 18:00 hrs** * Saturdays, **09:00 to 13:00 hrs** **Interested candidates:** Submit your CV via this platform or WhatsApp **55 4875 5124**. Job type: Full-time Salary: Up to $11,000.00 per month Benefits: * Employee discount * Option for an indefinite-term contract Work location: On-site employment

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 11,000/month

Senior Research Analyst - Oil Supply650956412788491225

Senior Research Analyst - Oil Supply

Wood Mackenzie is the global data and analytics business for the renewables, energy, and natural resources industries. Enhanced by technology. Enriched by human intelligence. In an ever\-changing world, companies and governments need reliable and actionable insight to lead the transition to a sustainable future. That’s why we cover the entire supply chain with unparalleled breadth and depth, backed by over 50 years’ experience. Our team of over 2,400 experts, operating across 30 global locations, are enabling customers’ decisions through real\-time analytics, consultancy, events and thought leadership. Together, we deliver the insight they need to separate risk from opportunity and make confident decisions when it matters most. **WoodMac.com** **Wood Mackenzie Brand Video** **Wood Mackenzie Values** * Inclusive – we succeed together * Trusting – we choose to trust each other * Customer committed – we put customers at the heart of our decisions * Future Focused – we accelerate change * Curious – we turn knowledge into action **Wood Mackenzie's Research** Wood Mackenzie’s research groups provide integrated subscription, research and advisory services to inform and support our client’s commercial and strategic decisions in the complex and rapidly changing energy industry across all sectors of the economy. Combining our deep knowledge of transport, battery technologies and raw material supply chains with our expertise in power, renewables, storage, and fuels modelling, and emerging technologies like hydrogen and CCUS, Wood Mackenzie can provide data and insight spanning the entire energy value chain. We cover supply chains, technology costs, policy and market issues, fundamentals\-based outlooks, scenario modelling, price forecasting, asset valuation, and commodity market landscapes. **Team Profile** Wood Mackenzie’s Oil Supply team provide granular analysis and commercial insight into global liquids supply in both the short and long\-term. The team sits within the Oil and Chemicals commodities group, but collaborates extensively across different teams, including upstream, downstream, chemicals and oil markets. Our oil supply analysis forms a key part of our integrated market outlooks, supporting our crude oil price outlooks. **Role Purpose** This role is for a **Senior Analyst** in the team, with the focus to analyse short\- and long\-term supply trends, both regionally and globally. We are seeking an enthusiastic candidate who is passionate about the future of the oil industry and how it will develop in the coming decades to meet the needs of society in a sustainable manner. Candidates will require an analytical mindset, an eye for detail, strong communication skills and have a flair for presenting to audiences \- both in small and large groups. The successful candidate will join a global team of world\-class industry experts undertaking industry\-leading fundamental research and modelling of all aspects of the oil and chemicals value chains. Our research and consulting services provide clients with unique insight into the future of the oil and refining sector and the markets which it serves, giving them a robust platform to make the best commercial and strategic decisions. The role offers the opportunity to develop modelling and forecasting techniques and industry knowledge through regular interaction with other members of the global Oils and Chemicals team. **Main Responsibilities** * Lead our short and long\-term supply analysis for specific regions, maintaining relevant data through secondary and primary research and that data quality, consistency and accuracy reflect market realities. * Work closely with colleagues in other Wood Mackenzie research teams to build a robust, integrated view of how supply will adapt through the energy transition. * Pro\-actively contribute to methodology and modelling improvements. * Present the outlook for regional supply to clients and prospects in meetings and via web\-calls where appropriate. * Work with the product managers of the evolving suite of oil market product offerings to deliver high quality content, which clearly communicates our analysis to clients. Contribute to development plans for the products, providing ideas and support for enhancements and improvements. * Respond to internal and external enquiries regarding oil supply in a timely and professional manner. * Work closely with the sales and marketing teams to service clients and grow the client base. **Knowledge and Experience** * You have demonstrable interest and relevant experience in the upstream oil sector. Experience as an engineer or analyst in oil market analysis would be a distinct advantage. * You have a knowledge of oil supply fundamentals with ability to develop and maintain short and long\-term models. * You have effective interpersonal and communication skills, including the presentation skills necessary to articulate your findings to industry participants at a range of levels. This is coupled with your ability to communicate highly complex and detailed market analysis, delivering messages that are easily understood. * You can learn established processes and procedures carefully, with attention to detail, while also an ability to improve and evolve current processes. * Strong analytical and problem\-solving capabilities. Interested in using both qualitative and quantitative methods to answer market questions. * Self\-driven. Capable of switching between the roles of an individual contributor and a collaborative leader. * Strong communication skills. Comfortable interacting with senior levels amongst customers and industry stakeholders. * Passionate, with a deep intellectual curiosity, about the energy and commodity industries. * Growth mindset, with a desire to develop yourself and others in the team. * Passion for using Artificial Intelligence and all the new analytical methods available to help us grow faster and better. * Strong excel skills required. Understanding of Python an advantage. **Equal Opportunities** We are an equal opportunities employer. This means we are committed to recruiting the best people regardless of their race, colour, religion, age, sex, national origin, disability or protected veteran status. You can find out more about your rights under the law at www.eeoc.gov If you are applying for a role and have a physical or mental disability, we will support you with your application or through the hiring process.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Industrial Maintenance Technician650956367837471226

Industrial Maintenance Technician

**Tornel Laboratories is seeking an Industrial Maintenance Technician in San Bartolo - Naucalpan de Juárez, State of Mexico** ------------------------------------------------------------------------------------------------------------------------- **TORNEL LABORATORIES** Tornel Laboratories, a 100% Mexican company, is dedicated to the care and well-being of animal health across small, medium, and large species. **We require:** **Electromechanical Technician, Maintenance** **Education:** * Technical degree in Electronics, Electromechanics, or Mechanical Engineering **Knowledge:** * Installations * Mechanical and electrical systems * Safety standards * Mechanical and electrical maintenance * Configuration and wiring of inductive, capacitive, and magnetic sensors * Maintenance of mechanical and hydraulic transmissions, pneumatic systems, and centrifugal pumps **Responsibilities:** * Perform scheduled or corrective maintenance tasks * Predictive and corrective maintenance on systems * Water-for-injection (WFI) distillers * Inspect and conduct routine tests on equipment and machinery * Clean and maintain HVAC systems (heating, ventilation, and air conditioning) * Conduct equipment inspection rounds **We offer:** * Salary: $12,000 monthly gross * 15 days’ Christmas bonus * 12 vacation days upon completion of one year * 25% vacation premium * $1,200 in grocery vouchers * Savings fund: 12.5 % * IMSS * Life insurance **Work location:** Naucalpan, State of Mexico - San Bartolo **Variable schedule:** Monday to Saturday **Desired education level:** Higher education - Degree holder **Desired experience level:** Intermediate **Departmental function:** Maintenance and repairs **Industry:** Pharmaceuticals **Skills:** * Responsible * Committed * Dynamic *This vacancy comes from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j_id=69691c88880000330092f86c&source=indeed*

Venustiano Carranza 27, Naucalpan Centro, 53000 Naucalpan de Juárez, Méx., Mexico

$MXN 12,000/year

Electronic Equipment Repair Technician650956366104351227

Electronic Equipment Repair Technician

**DIEBOLD NIXDORF DE MEXICO S.A. DE C.V. is seeking an Electronic Equipment Repair Technician at Lago Esmeralda - Atizapán de Zaragoza, State of Mexico** ------------------------------------------------------------------------------------------------------------------------------------------------------ **Summary of Responsibilities:** Repairs and tests mechanical and electromechanical assemblies and subassemblies. Works from drawings, sketches, wiring diagrams, and written or verbal instructions to understand and perform repair and/or testing activities. Ensures work complies with established technical, product, and quality requirements. Key Responsibilities: * Become familiar with Electronic Repair Technician practices and procedures. * Under guidance, performs routine Electronic Repair Technician tasks, including: identifying, isolating, and correcting product failures. * Disassembles, cleans, and refurbishes assigned product components. * Assists in performing tests, recording results, and reporting findings. Develops practical knowledge of DN product lines and associated diagnostic and test procedures. * Participates in regular product/repair/maintenance training (on-the-job, classroom, and online). * Learns and adheres to DN policies, electrostatic discharge (ESD) sensitivity requirements, and safety standards. * Learns and gains understanding of operational manuals, equipment capabilities, and manufacturer instructions. * Understands drawings, electrical schematics, and diagrams, as well as their use for diagnosing and resolving anomalies. * Assists in special projects as assigned. **Requirements:** * Education: Minimum of high school diploma or completed technical degree. * Experience: Minimum 0–2 years of experience in electronic equipment repair areas. (Professional internships or academic projects may be considered.) * Strong verbal and written communication skills. * Work location: Atizapán de Zaragoza, Esmeralda Zone. **Desired Education Level:** Upper Secondary **Desired Experience Level:** Entry Level **Departmental Function:** Maintenance and Repairs **Industry:** Manufacturing, Consumer Goods **Skills:** * Attention to Detail * Organization * Teamwork *This job posting originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j\_id\=696941cd6100002600947b28\&source\=indeed*

C. Pioneros del Cooperativismo 214, Mexico Nuevo, 52966 Cdad. López Mateos, Méx., Mexico

GENERAL MAINTENANCE TECHNICIAN650956365781791228

GENERAL MAINTENANCE TECHNICIAN

Skills and knowledge in: low-voltage electricity, air conditioning and refrigeration, finishing work, plumbing, carpentry, metalworking, general maintenance. Availability to work different shifts at shopping centers. Accustomed to working under pressure, complying with rules and policies. Valid driver’s license required; personal vehicle preferred. Gasoline allowance and basic vehicle maintenance support for personal vehicle. Food allowance. Bonus based on number of services and activities performed. Job type: Full-time Contact: 5567076123 Experience: minimum 2 years Education level: technical professional and/or high school Job type: Full-time, Contract-based Salary: $10,000.00 - $12,000.00 per month Job type: Full-time, Project-based or fixed-term, Probationary period Duration of contract: 3 months Salary: Starting from $10,000.00 per month Benefits: * Option for indefinite-term contract * Free uniforms Education: * Completed high school (Desirable) Experience: * Maintenance: 1 year (Desirable) * General maintenance: 1 year (Desirable) Work location: On-site employment

Av San Fernando 111, San Fernando, 52765 Naucalpan de Juárez, Méx., Mexico

$MXN 10,000-12,000/year

Backend Java Developer650956365000991229

Backend Java Developer

API's Developer **Job Description:** We are looking for an API Developer passionate about quality, speed of delivery, and teamwork. The ideal candidate must have experience developing high-performance API solutions, ensuring scalability, security, and process optimization, while also fostering continuous improvement and innovation within an agile environment. **Responsibilities:** * **Quality Development**: Build robust, scalable, and secure solutions with a strong focus on code quality. * **Speed of Delivery**: Meet established deadlines without compromising development quality. * **Team Collaboration**: Collaborate closely with other developers, designers, and project management teams. * **Optimization and Performance**: Improve API efficiency and performance through optimization practices. * **Innovation and Continuous Improvement**: Propose and implement improvements to processes and technologies used. * **Incident Management and Support**: Resolve technical incidents and provide timely support to ensure API operational continuity. **Functions:** * **Needs Identification**: Analyze user requirements and translate them into technical specifications. * **RESTful API Development**: Design and maintain efficient, scalable RESTful APIs. * **Data Integrity**: Ensure data quality and consistency across APIs. * **Technical Documentation Development**: Document processes, methodologies, and technical specifications. * **Security and Authentication Management**: Implement security mechanisms to protect APIs and data. * **API Maintenance and Support**: Provide ongoing support and perform enhancements on existing APIs. * **Production Deployment Monitoring**: Monitor and track production deployments. * **Quality Testing**: Conduct quality testing using various tools and methodologies. * **Technical Incident Management**: Address and manage technical incidents to ensure proper API functionality. **Technical Requirements:** **Intermediate Level:** * **Java 17+** / **Spring Boot** * **Swagger** * **Artifactory** * **Gradle / Maven** * **Git and GitLab** * **JUnit and Mockito** * **Postman** * **Artillery and JMeter** * **SonarQube** **Basic Level:** * **Docker** * **Oracle, PL/SQL, SQL (DDL, DML)** * **MongoDB** * **AWS (Elastic Container Service - ECS, CloudWatch, S3)** * **Jira** **Desired Skills:** * **Scalability and Maintainability**: Ensure APIs are scalable and easy to maintain over time. * **API Security Management**: Implement security best practices to protect data. * **Stakeholder and Client Collaboration**: Work effectively with clients and other stakeholders to identify needs and deliver appropriate solutions. * **Version and Deployment Management**: Manage versions and ensure correct API deployment. * **Testing and Code Quality**: Apply agile methodologies and automated testing to ensure delivered code quality. **We Offer:** * **Competitive salary** and additional benefits. * Opportunity to **work with cutting-edge technologies** in a dynamic team. * **Professional growth opportunities** and continuous training. * **Statutory benefits** * **SGMM** * **Work Mode: On-site** If you're passionate about technology and excited about API development, we want to meet you! **Send a WhatsApp message to 5516404825 with the job title “API's Developer”** Employment Type: Full-time Salary: $30,000.00 - $35,000.00 per month Benefits: * Major medical expense insurance Work Location: On-site employment

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 30,000-35,000/year

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